A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244556



Internal ID21311425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10739058..10756722hg38UCSC Ensembl
Outerchr9:10737968..10764097hg38UCSC Ensembl
Innerchr9:10739058..10756722hg19UCSC Ensembl
Outerchr9:10737968..10764097hg19UCSC Ensembl
Innerchr9:10729058..10746722hg18UCSC Ensembl
Outerchr9:10727968..10754097hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3826130
hg1926130
hg1826130
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169379
Supporting Variants
SamplesSNI_10
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244556
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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